Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,662 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,662 in last 12 months

Showing 13011320 of 49,990 recalls

Medical DeviceSeptember 16, 2025· Medtronic Sofamor Danek USA Inc

Recalled Item: Catalyft PL & PL40 Expandable Interbody System labeled as follows Recalled...

The Issue: Expandable interbody system cage may loose height or collapse (loss of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: SyncAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR...

The Issue: A software anomaly, under specific conditions when large rotational...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Spacelabs Healthcare, Ltd.

Recalled Item: Brand Name: Sentinel V11 Product Name: Sentinel V11 Model/Catalog Number:...

The Issue: Due to two distinct issues: 1. During patient admission, patient demographic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: Surgical Planner Recalled by Surgical Theater Inc Due to A software anomaly,...

The Issue: A software anomaly, under specific conditions when large rotational...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: SuRgical Planner (SRP) Recalled by Surgical Theater Inc Due to A software...

The Issue: A software anomaly, under specific conditions when large rotational...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: Endo Surgical Navigation Advanced Platform Patient Engagement (EndoSNAP)...

The Issue: A software anomaly, under specific conditions when large rotational...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: SpineAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR...

The Issue: A software anomaly, under specific conditions when large rotational...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: Surgical Navigation Advanced Platform (SNAP) Recalled by Surgical Theater...

The Issue: A software anomaly, under specific conditions when large rotational...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: Surgical Navigation Advanced Platform Patient Engagement (PE SNAP) Recalled...

The Issue: A software anomaly, under specific conditions when large rotational...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Abiomed, Inc.

Recalled Item: Automated Impella Controller (AIC) labeled as the following with...

The Issue: Potential for Automated Impella Controller (AIC) purge pressure issues due...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
DrugSeptember 15, 2025· Graviti Pharmaceuticals Private Limited

Recalled Item: Bupropion Hydrochloride Extended-Release Tablets USP (XL) Recalled by...

The Issue: Failed Tablet/Capsule Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 15, 2025· Amerisource Health Services LLC

Recalled Item: Carbamazepine Extended-Release Tablets Recalled by Amerisource Health...

The Issue: Failed Dissolution Specifications.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 15, 2025· Alcon Research LLC

Recalled Item: CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K Recalled by Alcon...

The Issue: XXX

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodSeptember 12, 2025· M.O.M Enterprises, LLC.

Recalled Item: Organic BABY bedtime drops Recalled by M.O.M Enterprises, LLC. Due to...

The Issue: Potential yeast contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· JB Chemicals and Pharmaceuticals Ltd

Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...

The Issue: Tablet/Capsules Imprinted with Wrong ID

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 12, 2025· JB Chemicals and Pharmaceuticals Ltd

Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...

The Issue: Tablet/Capsules Imprinted with Wrong ID

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund